New · posted Nov 11
Amgen · Biotechnology
Grad Intern - Global Patient Safety (Summer 2027)
- Remote, US
- Remote
- Internship
- Associate & Specialist
What you need
Basic Qualifications
Amgen requires that all individuals applying for a grad internship or a co-op assignment at Amgen must meet the following criteria:
- 18 years or older
- Graduated with a bachelor’s degree from an accredited college or university
- Currently enrolled in an MBA program for an MBA internship OR a Master’s program for a Master’s internship OR a PharmD program for a PharmD internship OR Ph.D. for a PhD internship from an accredited college or university and completion of the first year of MBA OR Master’s OR Pharm D OR Ph.D. program before the internship starts
Program Eligibility Requirements
- Must be available to work a full-time schedule.
- Expected continued enrollment in an accredited college or university following the internship program / co-op
- Student must be located in the United States for the duration of the internship program
What We Expect of You
We are all different, yet we all use our unique contributions to serve patients.The highly motivated individual we seek is a collaborative and intellectually curious professional with these qualifications::
Preferred Qualificationsnice to have
- Degree concentration(s): Pharmacy
- Excellent written and verbal communication skills.
- Ability to work independently and collaboratively within cross-functional teams.
- Proficiency in Microsoft Office (Word, PowerPoint, Excel).·
- Prior experience in clinical research (coursework, clerkships, projects) and/or clinical pharmacy.
- Familiarity with clinical trial processes or regulatory documentation.
- Strong interest in pursuing a career in the pharmaceutical or biotechnology industry.
What you'll do
Let’s do this. Let’s change the world. During this program, you will work with the Late-Stage Oncology Clinical Science team to support the execution of oncology clinical trials. You will gain hands-on experience in clinical data review, study conduct, and cross-functional collaboration while contributing to activities that support the development of innovative therapies for patients with cancer. The key responsibilities:
· Support clinical development of oncology compounds and assist with day-to-day execution of clinical trials, focusing on data quality.
· Participate in cross-functional discussions involving clinical, statistics, operations, and data management teams.
· Support clinical trial operations by preparing documents such as literature reviews, slide decks, and tracking study progress.
· Learn about and maintain study data quality by performing data review and identifying clinical findings.
· Conduct background research on oncology disease states, treatments, or trial methodologies to support clinical projects.
· Contribute to scientific communication by assisting in preparation of internal presentations and literature summaries.
· Learn about the clinical scientist role in oncology clinical development through meetings, mentorship, and guided projects.
Pay and benefits
$74,000 – $86,000 a year
Employer providedUSD - USD
What You Can Expect of Us
Build a network of colleagues that will endure and grow throughout your time with us and beyond.
Bring your authentic self to the table and become the professional you’re inspired to be through accepting a culture that values the diversity of thought and experience and will flex to your strengths and possibilities.
Participate in executive and social networking events, as well as community volunteer projects.
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
The base pay range for this opportunity in the U.S. is $35.34 – $41.20 per hour.
Working conditions
Career Category
College Job
careers.amgen.com - Please search for Keyword R-260757
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Sponsorship
Candidates must be authorized to work in the U.S. for the duration of this program. Sponsorship for future FTE roles is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
From the posting
About Amgen
Join Amgen’s Mission of Serving Patients
At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.
Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Equal opportunity, accessibility and legal noticesAmgen's statements, word for word
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Job intelligence
The context around this role
Live data · November 11, 2026
Salary intelligence
How the pay compares
This role's midpoint is level with the US median for Clinical Development roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US5 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $74,000 | — | $86,000 |
| All US (middle half) | $71,500 | $80,000 | $86,000 |
This role: Amgen's own published range. Comparisons: the base pay employers published on open Clinical Development roles at the same level on Regulatory Jobs, November 11, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Development
The general path across 296 open Clinical Development roles on Regulatory Jobs, with the titles they carry most. Not Amgen's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 23 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership7
- Clinical trial conduct6
- Documentation and SOPs4
- Data and digital systems2
- Lab testing and methods1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Clinical Development work in biotechnology, each linked to the agency or standards body that publishes it.
- ICHICH E6(R3) good clinical practice(official source, opens in a new tab)The international standard for the design, conduct and reporting of clinical trials
- FDA21 CFR Part 312(official source, opens in a new tab)Investigational New Drug applications and sponsor duties in drug trials
- FDA21 CFR Part 50(official source, opens in a new tab)Protection of human subjects: informed consent in FDA-regulated trials
- FDA21 CFR Part 56(official source, opens in a new tab)Institutional review boards for FDA-regulated clinical investigations
- FDAFDA study data standards(official source, opens in a new tab)Required data standards and technical conformance for clinical study data
- EUEU Clinical Trials Regulation 536/2014(official source, opens in a new tab)How clinical trials of medicines are authorized and run in the EU, through CTIS
- ICHICH E8(R1)(official source, opens in a new tab)General considerations for clinical studies and quality by design in trials
- HHS45 CFR Part 46 (Common Rule)(official source, opens in a new tab)The federal policy for the protection of human research subjects
- NIH42 CFR Part 11(official source, opens in a new tab)Clinical trial registration and results reporting on ClinicalTrials.gov
- FDAFDA Bioresearch Monitoring (BIMO)(official source, opens in a new tab)FDA inspections of clinical investigators, sponsors, IRBs and GLP labs
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- HHSHIPAA Privacy Rule(official source, opens in a new tab)Federal protections for individually identifiable health information
- EUGDPR (Regulation 2016/679)(official source, opens in a new tab)The EU General Data Protection Regulation for personal data, including health data
- ICHICH E9 and E9(R1)(official source, opens in a new tab)Statistical principles for clinical trials and estimands
- FDA21 CFR 314.80 and 600.80(official source, opens in a new tab)Postmarketing reporting of adverse drug and biologic experiences
- ICHICH E2A to E2F(official source, opens in a new tab)Clinical safety data management, expedited reporting and periodic safety reports
Company hiring pulse
Amgen on Regulatory Jobs
- 60
- Open roles
- 60
- Distinct roles
- 5
- Locations
By discipline
- Quality35 57%
- Regulatory13 21%
- Clinical13 21%
By level
- Manager20 33%
- Senior & Principal19 31%
- Director13 21%
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Grad Intern - Global Patient Safety (Summer 2027) at Amgen
Open until filled. $74K–$86K a year, employer provided.